Difference between revisions of "Waldenström macroglobulinemia"

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m (Text replace - ", et al. " to " et al. ")
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BDR: '''<u>B</u>'''ortezomib, '''<u>D</u>'''examethasone, '''<u>R</u>'''ituximab
 
BDR: '''<u>B</u>'''ortezomib, '''<u>D</u>'''examethasone, '''<u>R</u>'''ituximab
  
−
===Regimen, Treon et al. 2009 (WMCTG 05-180)===
+
===Regimen #1, Treon et al. 2009 (WMCTG 05-180)===
−
Level of Evidence:
 
 
<span  
 
<span  
 
style="background:#EEEE00;
 
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*[[Dexamethasone (Decadron)]] 40 mg IV once per day on days 1, 4, 8, 11
 
*[[Dexamethasone (Decadron)]] 40 mg IV once per day on days 1, 4, 8, 11
 
*[[Rituximab (Rituxan)]] 375 mg/m2 IV once on day 11
 
*[[Rituximab (Rituxan)]] 375 mg/m2 IV once on day 11
−
 
−
'''"four continuous cycles of BDR followed by a 12-week pause and then four additional cycles of BDR spaced 12 weeks apart"''' in hopes of reducing the incidence of peripheral neuropathy.  The length of the initial cycles was not specified in the paper.
 
  
 
Supportive medications:
 
Supportive medications:
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*"The use of diphenhydramine, acetaminophen and, at the treating physician's discretion, corticosteroids and/or ranitidine or cimetidine was permitted for rituximab infusion prophylaxis. Granulocyte colony-stimulating factor, erythropoietin, and transfusions of packed RBCs or platelets were permitted to support patient's counts during therapy."
 
*"The use of diphenhydramine, acetaminophen and, at the treating physician's discretion, corticosteroids and/or ranitidine or cimetidine was permitted for rituximab infusion prophylaxis. Granulocyte colony-stimulating factor, erythropoietin, and transfusions of packed RBCs or platelets were permitted to support patient's counts during therapy."
 
*"The prophylactic use of plasmapheresis was recommended for patients demonstrating an IgM level of ≥ 5,000 mg/dL before the administration of rituximab, given the potential for rituximab-mediated IgM flare and aggravation of hyperviscosity."
 
*"The prophylactic use of plasmapheresis was recommended for patients demonstrating an IgM level of ≥ 5,000 mg/dL before the administration of rituximab, given the potential for rituximab-mediated IgM flare and aggravation of hyperviscosity."
 +
 +
'''"four continuous cycles of BDR followed by a 12-week pause and then four additional cycles of BDR spaced 12 weeks apart"''' in hopes of reducing the incidence of peripheral neuropathy.  The length of the initial cycles was not specified in the paper.
 +
 +
===Regimen #2, Dimopoulos et al. 2013===
 +
<span
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padding:3px 6px 3px 6px;
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border-color:black;
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border-style:solid;">Phase II</span>
 +
 +
*[[Bortezomib (Velcade)]] 1.3 mg/m2 IV once per day on days 1, 4, 8, 11
 +
 +
'''21-day cycle, followed by:'''
 +
 +
*[[Bortezomib (Velcade)]] 1.6 mg/m2 IV once per week on days 1, 8, 15, 22
 +
*[[Dexamethasone (Decadron)]] 40 mg IV once per week on days 1, 8, 15, 22, cycles 2 and 5 only
 +
*[[Rituximab (Rituxan)]] 375 mg/m2 IV once per week on days 1, 8, 15, 22, cycles 2 and 5 only
 +
 +
Supportive medications:
 +
*[[Acetaminophen (Tylenol)]] 1000 mg PO once prior to [[Rituximab (Rituxan)]] infusions
 +
*[[Diphenhydramine (Benadryl)]] 50 mg IV once prior to [[Rituximab (Rituxan)]] infusions
 +
**[[Valacyclovir (Valtrex)]] dose not specified or [[Acyclovir (Zovirax)]] dose not specified mandated for VZV prophylaxis
 +
 +
'''21-day cycle x 4 cycles (5 cycles, overall)'''
  
 
===References===
 
===References===
−
# Treon SP, Ioakimidis L, Soumerai JD, Patterson CJ, Sheehy P, Nelson M, Willen M, Matous J, Mattern J 2nd, Diener JG, Keogh GP, Myers TJ, Boral A, Birner A, Esseltine DL, Ghobrial IM. Primary therapy of Waldenström macroglobulinemia with  bortezomib, dexamethasone, and rituximab: WMCTG clinical trial 05-180. J Clin Oncol. 2009 Aug 10;27(23):3830-5. doi: 10.1200/JCO.2008.20.4677. Epub 2009 Jun 8. [http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2727288/ link to original article] '''contains verified protocol''' [http://www.ncbi.nlm.nih.gov/pubmed/19506160 PubMed]  
+
# Treon SP, Ioakimidis L, Soumerai JD, Patterson CJ, Sheehy P, Nelson M, Willen M, Matous J, Mattern J 2nd, Diener JG, Keogh GP, Myers TJ, Boral A, Birner A, Esseltine DL, Ghobrial IM. Primary therapy of Waldenström macroglobulinemia with  bortezomib, dexamethasone, and rituximab: WMCTG clinical trial 05-180. J Clin Oncol. 2009 Aug 10;27(23):3830-5. doi: 10.1200/JCO.2008.20.4677. Epub 2009 Jun 8. [http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2727288/ link to original article] '''contains verified protocol''' [http://www.ncbi.nlm.nih.gov/pubmed/19506160 PubMed]
 +
# Dimopoulos MA, García-Sanz R, Gavriatopoulou M, Morel P, Kyrtsonis MC, Michalis E, Kartasis Z, Leleu X, Palladini G, Tedeschi A, Gika D, Merlini G, Kastritis E, Sonneveld P. Primary therapy of Waldenstrom's macroglobulinemia (WM) with weekly bortezomib, low-dose dexamethasone and rituximab (BDR): long term results of a phase II study of the European Myeloma Network (EMN). Blood. 2013 Sep 4. [Epub ahead of print] [http://bloodjournal.hematologylibrary.org/content/122/19/3276.full link to original article] '''contains verified protocol''' [http://www.ncbi.nlm.nih.gov/pubmed/24004667 PubMed]
  
 
==Bortezomib & Rituximab==
 
==Bortezomib & Rituximab==
  
 
===Regimen, Ghobrial et al. 2010===
 
===Regimen, Ghobrial et al. 2010===
−
Level of Evidence:
 
 
<span  
 
<span  
 
style="background:#EEEE00;
 
style="background:#EEEE00;
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*[[Bortezomib (Velcade)]] 1.6 mg/m2 IV once per day on days 1, 8, 15
 
*[[Bortezomib (Velcade)]] 1.6 mg/m2 IV once per day on days 1, 8, 15
 
*[[Rituximab (Rituxan)]] 375 mg/m2 IV once per day on days 1, 8, 15, 22 of cycles 1 and 4 only
 
*[[Rituximab (Rituxan)]] 375 mg/m2 IV once per day on days 1, 8, 15, 22 of cycles 1 and 4 only
−
 
−
'''28-day cycles x up to 6 cycles'''
 
  
 
Supportive medications:
 
Supportive medications:
 
*"Antiviral prophylaxis was recommended in all patients prior to initiation of therapy and for 3 months after completion of the six cycles."
 
*"Antiviral prophylaxis was recommended in all patients prior to initiation of therapy and for 3 months after completion of the six cycles."
 +
 +
'''28-day cycles x up to 6 cycles'''
  
 
===References===
 
===References===
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===Regimen, Leblond et al. 2013===
 
===Regimen, Leblond et al. 2013===
−
Level of Evidence:
 
 
<span  
 
<span  
 
style="background:#00CD00;
 
style="background:#00CD00;
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*[[Chlorambucil (Leukeran)]] 8 mg/m2 (6 mg/m2 per day if older than 75 years old) PO daily on days 1 to 10
 
*[[Chlorambucil (Leukeran)]] 8 mg/m2 (6 mg/m2 per day if older than 75 years old) PO daily on days 1 to 10
−
 
−
'''28-day cycles x up to 12 cycles'''
 
  
 
Supportive medications:
 
Supportive medications:
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**[[Trimethoprim/Sulfamethoxazole (Bactrim DS)|Trimethoprim/Sulfamethoxazole (Bactrim SS)]] 1 tablet PO once daily  
 
**[[Trimethoprim/Sulfamethoxazole (Bactrim DS)|Trimethoprim/Sulfamethoxazole (Bactrim SS)]] 1 tablet PO once daily  
 
**[[Pentamidine (Nebupent)]] 300 mg inhaled once per month
 
**[[Pentamidine (Nebupent)]] 300 mg inhaled once per month
 +
 +
'''28-day cycles x up to 12 cycles'''
  
 
===References===
 
===References===
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===Regimen, Laszlo et al. 2010===
 
===Regimen, Laszlo et al. 2010===
−
Level of Evidence:
 
 
<span  
 
<span  
 
style="background:#EEEE00;
 
style="background:#EEEE00;
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===Regimen===
 
===Regimen===
−
Level of Evidence:
 
 
<span  
 
<span  
 
style="background:#00CD00;
 
style="background:#00CD00;
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*[[Fludarabine (Fludara)]] 40 mg/m2 (30 mg/m2 per day if older than 75 years old) PO once daily on days 1 to 5
 
*[[Fludarabine (Fludara)]] 40 mg/m2 (30 mg/m2 per day if older than 75 years old) PO once daily on days 1 to 5
−
 
−
'''28-day cycles x up to 6 cycles'''
 
  
 
Supportive medications:
 
Supportive medications:
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**[[Valacyclovir (Valtrex)]] 500 mg PO once daily  
 
**[[Valacyclovir (Valtrex)]] 500 mg PO once daily  
 
**[[Acyclovir (Zovirax)]] 200-400 mg PO BID  
 
**[[Acyclovir (Zovirax)]] 200-400 mg PO BID  
 +
 +
'''28-day cycles x up to 6 cycles'''
  
 
===References===
 
===References===
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===Regimen, Ghobrial et al. 2010===
 
===Regimen, Ghobrial et al. 2010===
−
Level of Evidence:
 
 
<span  
 
<span  
 
style="background:#EEEE00;
 
style="background:#EEEE00;
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*[[Bortezomib (Velcade)]] 1.6 mg/m2 IV once per day on days 1, 8, 15
 
*[[Bortezomib (Velcade)]] 1.6 mg/m2 IV once per day on days 1, 8, 15
 
*[[Rituximab (Rituxan)]] 375 mg/m2 IV once per day on days 1, 8, 15, 22 of cycles 1 and 4 only
 
*[[Rituximab (Rituxan)]] 375 mg/m2 IV once per day on days 1, 8, 15, 22 of cycles 1 and 4 only
−
 
−
'''28-day cycles x up to 6 cycles'''
 
  
 
Supportive medications:
 
Supportive medications:
 
*"At the time of initiation of the study, the incidence of herpes zoster reactivation with bortezomib in WM was not well documented; therefore, antiviral prophylaxis was not mandated."
 
*"At the time of initiation of the study, the incidence of herpes zoster reactivation with bortezomib in WM was not well documented; therefore, antiviral prophylaxis was not mandated."
 +
 +
'''28-day cycles x up to 6 cycles'''
  
 
===References===
 
===References===
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===Regimen, Rummel et al. 2005===
 
===Regimen, Rummel et al. 2005===
−
Level of Evidence:
 
 
<span  
 
<span  
 
style="background:#ff0000;
 
style="background:#ff0000;
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*[[Rituximab (Rituxan)]] 375 mg/m2 IV once on day 1
 
*[[Rituximab (Rituxan)]] 375 mg/m2 IV once on day 1
  
−
'''Cycle 1 is started 7 days after the first dose of rituximab'''
+
'''Cycle 1 is started 7 days after the first dose of rituximab:'''
  
 
*[[Bendamustine (Treanda)]] 90 mg/m2 IV over 30 minutes once on days 1 & 2 of cycles 1 to 4
 
*[[Bendamustine (Treanda)]] 90 mg/m2 IV over 30 minutes once on days 1 & 2 of cycles 1 to 4
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===Regimen, Laszlo et al. 2010===
 
===Regimen, Laszlo et al. 2010===
−
Level of Evidence:
 
 
<span  
 
<span  
 
style="background:#EEEE00;
 
style="background:#EEEE00;
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==Everolimus==
 
==Everolimus==
 
===Regimen, Ghobrial et al. 2010===
 
===Regimen, Ghobrial et al. 2010===
−
Level of Evidence:
 
 
<span  
 
<span  
 
style="background:#EEEE00;
 
style="background:#EEEE00;
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*[[Everolimus (Afinitor)]] 10 mg PO once per day while fasting
 
*[[Everolimus (Afinitor)]] 10 mg PO once per day while fasting
−
 
−
'''28-day cycles, given until progression or unacceptable toxicity'''
 
  
 
Supportive medications:
 
Supportive medications:
 
*WBC growth factors per physician discretion if neutropenia occurred, but it was not to be used prophylactically in order to maintain dosing.
 
*WBC growth factors per physician discretion if neutropenia occurred, but it was not to be used prophylactically in order to maintain dosing.
 
*Erythropoietin for anemia allowed per physician discretion.
 
*Erythropoietin for anemia allowed per physician discretion.
 +
 +
'''28-day cycles, given until progression or unacceptable toxicity'''
  
 
===References===
 
===References===
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==Panobinostat==
 
==Panobinostat==
 
===Regimen, Ghobrial et al. 2013===
 
===Regimen, Ghobrial et al. 2013===
−
Level of Evidence:
 
 
<span  
 
<span  
 
style="background:#EEEE00;
 
style="background:#EEEE00;

Revision as of 22:28, 7 November 2013

Use of this site is subject to you reading and agreeing with the terms set forth in the disclaimer.

Is there a regimen missing from this list? Would you like to share a different dosage/schedule or an additional reference for a regimen? Have you noticed an error? Do you have an idea that will help the site grow to better meet your needs and the needs of many others? You are invited to contribute to the site.


Untreated

BDR

BDR: Bortezomib, Dexamethasone, Rituximab

Regimen #1, Treon et al. 2009 (WMCTG 05-180)

Phase II

Treon et al. 2009 did not clearly indicate the schedule for bortezomib, but it is inferred that this is what was meant.

Supportive medications:

  • Valacyclovir (Valtrex) 1 g PO once per day or Acyclovir (Zovirax) 400 mg PO twice per day recommended for shingles prophylaxis
  • "The use of diphenhydramine, acetaminophen and, at the treating physician's discretion, corticosteroids and/or ranitidine or cimetidine was permitted for rituximab infusion prophylaxis. Granulocyte colony-stimulating factor, erythropoietin, and transfusions of packed RBCs or platelets were permitted to support patient's counts during therapy."
  • "The prophylactic use of plasmapheresis was recommended for patients demonstrating an IgM level of ≥ 5,000 mg/dL before the administration of rituximab, given the potential for rituximab-mediated IgM flare and aggravation of hyperviscosity."

"four continuous cycles of BDR followed by a 12-week pause and then four additional cycles of BDR spaced 12 weeks apart" in hopes of reducing the incidence of peripheral neuropathy. The length of the initial cycles was not specified in the paper.

Regimen #2, Dimopoulos et al. 2013

Phase II

21-day cycle, followed by:

Supportive medications:

21-day cycle x 4 cycles (5 cycles, overall)

References

  1. Treon SP, Ioakimidis L, Soumerai JD, Patterson CJ, Sheehy P, Nelson M, Willen M, Matous J, Mattern J 2nd, Diener JG, Keogh GP, Myers TJ, Boral A, Birner A, Esseltine DL, Ghobrial IM. Primary therapy of Waldenström macroglobulinemia with bortezomib, dexamethasone, and rituximab: WMCTG clinical trial 05-180. J Clin Oncol. 2009 Aug 10;27(23):3830-5. doi: 10.1200/JCO.2008.20.4677. Epub 2009 Jun 8. link to original article contains verified protocol PubMed
  2. Dimopoulos MA, García-Sanz R, Gavriatopoulou M, Morel P, Kyrtsonis MC, Michalis E, Kartasis Z, Leleu X, Palladini G, Tedeschi A, Gika D, Merlini G, Kastritis E, Sonneveld P. Primary therapy of Waldenstrom's macroglobulinemia (WM) with weekly bortezomib, low-dose dexamethasone and rituximab (BDR): long term results of a phase II study of the European Myeloma Network (EMN). Blood. 2013 Sep 4. [Epub ahead of print] link to original article contains verified protocol PubMed

Bortezomib & Rituximab

Regimen, Ghobrial et al. 2010

Phase II

Supportive medications:

  • "Antiviral prophylaxis was recommended in all patients prior to initiation of therapy and for 3 months after completion of the six cycles."

28-day cycles x up to 6 cycles

References

  1. Ghobrial IM, Xie W, Padmanabhan S, Badros A, Rourke M, Leduc R, Chuma S, Kunsman J, Warren D, Poon T, Harris B, Sam A, Anderson KC, Richardson PG, Treon SP, Weller E, Matous J. Phase II trial of weekly bortezomib in combination with rituximab in untreated patients with Waldenström Macroglobulinemia. Am J Hematol. 2010 Sep;85(9):670-4. doi: 10.1002/ajh.21788. link to original article contains verified protocol PubMed

Chlorambucil (Leukeran)

Regimen, Leblond et al. 2013

Phase III

Supportive medications:

28-day cycles x up to 12 cycles

References

  1. Leblond V, Johnson S, Chevret S, Copplestone A, Rule S, Tournilhac O, Seymour JF, Patmore RD, Wright D, Morel P, Dilhuydy MS, Willoughby S, Dartigeas C, Malphettes M, Royer B, Ewings M, Pratt G, Lejeune J, Nguyen-Khac F, Choquet S, Owen RG. Results of a randomized trial of chlorambucil versus fludarabine for patients with untreated waldenstrom macroglobulinemia, marginal zone lymphoma, or lymphoplasmacytic lymphoma. J Clin Oncol. 2013 Jan 20;31(3):301-7. Epub 2012 Dec 10. link to original article contains verified protocol PubMed

Cladribine & Rituximab

Regimen, Laszlo et al. 2010

Phase II

Monthly cycles x 4 cycles

References

  1. Laszlo D, Andreola G, Rigacci L, Fabbri A, Rabascio C, Mancuso P, Pruneri G, Radice D, Pinto A, Frigeri F, Calabrese L, Billio A, Bertolini F, Martinelli G. Rituximab and subcutaneous 2-chloro-2'-deoxyadenosine combination treatment for patients with Waldenstrom macroglobulinemia: clinical and biologic results of a phase II multicenter study. J Clin Oncol. 2010 May 1;28(13):2233-8. Epub 2010 Apr 5. link to original article contains verified protocol PubMed

Fludarabine (Fludara)

Regimen

Phase III

  • Fludarabine (Fludara) 40 mg/m2 (30 mg/m2 per day if older than 75 years old) PO once daily on days 1 to 5

Supportive medications:

28-day cycles x up to 6 cycles

References

  1. Leblond V, Johnson S, Chevret S, Copplestone A, Rule S, Tournilhac O, Seymour JF, Patmore RD, Wright D, Morel P, Dilhuydy MS, Willoughby S, Dartigeas C, Malphettes M, Royer B, Ewings M, Pratt G, Lejeune J, Nguyen-Khac F, Choquet S, Owen RG. Results of a randomized trial of chlorambucil versus fludarabine for patients with untreated waldenstrom macroglobulinemia, marginal zone lymphoma, or lymphoplasmacytic lymphoma. J Clin Oncol. 2013 Jan 20;31(3):301-7. doi:10.1200/JCO.2012.44.7920. Epub 2012 Dec 10. link to original article contains verified protocol PubMed

Relapsed/refractory

Bortezomib & Rituximab

Regimen, Ghobrial et al. 2010

Phase II

Supportive medications:

  • "At the time of initiation of the study, the incidence of herpes zoster reactivation with bortezomib in WM was not well documented; therefore, antiviral prophylaxis was not mandated."

28-day cycles x up to 6 cycles

References

  1. Ghobrial IM, Hong F, Padmanabhan S, Badros A, Rourke M, Leduc R, Chuma S, Kunsman J, Warren D, Harris B, Sam A, Anderson KC, Richardson PG, Treon SP, Weller E, Matous J. Phase II trial of weekly bortezomib in combination with rituximab in relapsed or relapsed and refractory Waldenstrom macroglobulinemia. J Clin Oncol. 2010 Mar 10;28(8):1422-8. doi: 10.1200/JCO.2009.25.3237. Epub 2010 Feb 8. link to original article contains verified protocol PubMed

BR

BR: Bendamustine, Rituximab

Regimen, Rummel et al. 2005

Phase II, <20 patients reported

Cycle 1 is started 7 days after the first dose of rituximab:

28-day cycles x 5 cycles

References

  1. Rummel MJ, Al-Batran SE, Kim SZ, Welslau M, Hecker R, Kofahl-Krause D, Josten KM, Dürk H, Rost A, Neise M, von Grünhagen U, Chow KU, Hansmann ML, Hoelzer D, Mitrou PS. Bendamustine plus rituximab is effective and has a favorable toxicity profile in the treatment of mantle cell and low-grade non-Hodgkin's lymphoma. J Clin Oncol. 2005 May 20;23(15):3383-9. link to original article contains protocol PubMed

Cladribine & Rituximab

Regimen, Laszlo et al. 2010

Phase II

Monthly cycles x 4 cycles

References

  1. Laszlo D, Andreola G, Rigacci L, Fabbri A, Rabascio C, Mancuso P, Pruneri G, Radice D, Pinto A, Frigeri F, Calabrese L, Billio A, Bertolini F, Martinelli G. Rituximab and subcutaneous 2-chloro-2'-deoxyadenosine combination treatment for patients with Waldenstrom macroglobulinemia: clinical and biologic results of a phase II multicenter study. J Clin Oncol. 2010 May 1;28(13):2233-8. Epub 2010 Apr 5. link to original article contains verified protocol PubMed

Everolimus

Regimen, Ghobrial et al. 2010

Phase II

Supportive medications:

  • WBC growth factors per physician discretion if neutropenia occurred, but it was not to be used prophylactically in order to maintain dosing.
  • Erythropoietin for anemia allowed per physician discretion.

28-day cycles, given until progression or unacceptable toxicity

References

  1. Ghobrial IM, Gertz M, Laplant B, Camoriano J, Hayman S, Lacy M, Chuma S, Harris B, Leduc R, Rourke M, Ansell SM, Deangelo D, Dispenzieri A, Bergsagel L, Reeder C, Anderson KC, Richardson PG, Treon SP, Witzig TE. Phase II trial of the oral mammalian target of rapamycin inhibitor everolimus in relapsed or refractory Waldenstrom macroglobulinemia. J Clin Oncol. 2010 Mar 10;28(8):1408-14. doi:10.1200/JCO.2009.24.0994. Epub 2010 Feb 8. link to original article contains verified protocol PubMed

Panobinostat

Regimen, Ghobrial et al. 2013

Phase II

28-day cycles, given until progression of disease

References

  1. Ghobrial IM, Campigotto F, Murphy TJ, Boswell EN, Banwait R, Azab F, Chuma S, Kunsman J, Donovan A, Masood F, Warren D, Rodig S, Anderson KC, Richardson PG, Weller E, Matous J. Results of a phase 2 trial of the single-agent histone deacetylase inhibitor panobinostat in patients with relapsed/refractory Waldenstrom macroglobulinemia. Blood. 2013 Feb 21;121(8):1296-303. doi:10.1182/blood-2012-06-439307. Epub 2013 Jan 3. link to original article contains verified protocol PubMed
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